BOLEST DEPONOVANJA IMUNOGLOBULINA G4 (IgG4) I GRANULOMATOZA SA POLIANGTISOM KOD DECE: PRIKAZ BOLESNIKA SA NOVIM SINDROMOM PREKLAPANJA
Sažetak
Granulomatoza sa poliangitisom, prethodno nazivana Wegenerova granulomatoza, jedan je od glavnih oblika vaskulitisa udruženih sa antitelima protiv citoplazme neutrofila (engl. anti-neutrophil cytoplasm antibody ‒ ANCA) i najčešći vaskulitis malih i srednjih krvnih sudova kod dece. Bolest deponovanja imunoglobulina G4 (IgG4) karakteriše se inflamatornim pseudotumorima uz povišene vrednosti IgG4 u serumu. Pseudotumor orbite kod dece može biti inicijalna klinička prezentacija obaju pomenutih entiteta. U radu je prikazana devojčica sa neuobičajenom pojavom novog sindroma preklapanja ovih dvaju entiteta, koja se inicijalno prezentovala pseudotumorom orbite. Takođe, predstavljeni su izazovi dijagnostičkog postupka i primenjena terapija.
Reference
Ahmed M, Niffenegger JH, Jakobiec FA, Ben-Arie-Weintrob Y, Gion N, Androudi S, et al. Diagnosis of limited ophthalmic Wegener granulomatosis: distinctive pathologic features with ANCA test confirmation. Int Ophthalmol 2008; 28(1): 35-46. [CrossRef] [Pubmed]
Aletaha M, Tavakoli M, Rezaei Kanavi M, Hashemlou A, Roghaei S. Bilateral orbital mass lesions: a presentation of Wegener’s granulomatosis. J Ophthalmic Vis Res 2011; 6: 215-8. [Pubmed]
Bohm M, Gonzalez Fernandez MI, Ozen S, Pistorio A, Dolezalova P, Brogan P, et al. Clinical features of childhood granulomatosis with polyangiitis (wegener's granulomatosis). Pediatr Rheumatol Online J 2014; 12: 18. [CrossRef] [Pubmed]
Cabral DA, Canter DL, Muscal E, Nanda K, Wahezi DM, Spalding SJ, et al. Comparing Presenting Clinical Features in 48 Children With Microscopic Polyangiitis to 183 Children Who Have Granulomatosis With Polyangiitis (Wegener's): An ARChiVe Cohort Study. Arthritis Rheumatol 2016; 68(10): 2514-26. [CrossRef] [Pubmed]
Casssidy JT, Petty RE, Laxer RM, Lindsley CB. Textbook of pediatric rheumatology. Sixth edition ed. Philadelphia, USA: W.B.Saunders Company; 2010.
Chang SY, Keogh K, Lewis JE, Ryu JH, Yi ES. Increased IgG4-Positive Plasma Cells in Granulomatosis with Polyangiitis: A Diagnostic Pitfall of IgG4-Related Disease. Int J Rheumatol 2012; 2012: 121702. [CrossRef] [Pubmed]
Danlos FX, Rossi GM, Blockmans D, Emmi G, Kronbichler A, Durupt S, et al. French Vasculitis Study Group. Antineutrophil cytoplasmic antibody-associated vasculitides and IgG4-related disease: A new overlap syndrome. Autoimmun Rev 2017; 16(10): 1036-43. [CrossRef] [Pubmed]
Demir AM, Aydin F, Acar B, Kurt T, Poyraz A, Kiremitci S, et al. IgG4-related disease and ANCA positive vasculitis in childhood: a case-based review. Clin Rheumatol 2021; 40(9): 3817-25. [CrossRef] [Pubmed]
Drobysheva A, Fuller J, Pfeifer CM, Rakheja D. Orbital Granulomatosis With Polyangiitis Mimicking IgG4-Related Disease in a 12-Year-Old Male. Int J Surg Pathol 2018; 26(5): 453-8. [CrossRef] [Pubmed]
Erden A, Bolek EC, Yardimci KG, Kilic L, Bilgen SA, Karadag O. Do ANCA‐associated vasculitides and IgG4‐related disease really overlap or not?. Int J Rheum Dis 2019; 22(10): 1926-32. [CrossRef] [Pubmed]
Hamano H, Kawa S, Horiuchi A, Unno H, Furuya N, Akamatsu T, et al. High serum IgG4 concentrations in patients with sclerosing pancreatitis. N Engl J Med 2001; 344(10): 732-8. [CrossRef] [Pubmed]
Holland M, Hewins P, Goodall M, Adu D, Jefferis R, Savage CO. Anti‐neutrophil cytoplasm antibody IgG subclasses in Wegener's granulomatosis: a possible pathogenic role for the IgG4 subclass. Clin Exp Immunol 2004; 138(1): 183‐92. [CrossRef] [Pubmed]
James KE, Xiao R, Merkel PA, Weiss PF. Clinical course and outcomes of childhood-onset granulomatosis with polyangiitis. Clin Exp Rheumatol 2017; 35(suppl 103)(1): 202-8. [Pubmed]
Jennette JC, Falk RJ, Bacon PA, Bass N, Cid MC, Ferrario F, et al. 2012 revised International Chapel Hill Consensus Conference Nomenclature of Vasculitides. Arthritis Rheum 2013; 65(1): 1-11. [Pubmed]
Karim F, Loeffen J, Bramer W, Westenberg L, Verdijk R, van Hagen M, et al. IgG4-related disease: a systematic review of this unrecognized disease in pediatrics. Pediatr Rheumatol Online J 2016; 14(1): 18. [CrossRef] [Pubmed]
Kawashima H, Utsugi A, Shibamiya A, Iida K, Mimura N, Ohashi H, et al. Consideration concerning similarities and differences between ANCA-associated vasculitis and IgG-4-related diseases: case series and review of literature. Immunol Res 2019; 67(1): 99-107. [CrossRef] [Pubmed]
Kaya Akca Ü, Atalay E, Kasap Cüceoğlu M, Şener S, Balık Z, Başaran Ö, et al. IgG4-related disease in pediatric patients: a single-center experience. Rheumatol Int 2022; 42(7): 1177-85. [CrossRef] [Pubmed]
Lanzillotta M, Mancuso G, Della-Torre E. Advances in the diagnosis and management of IgG4 related disease. BMJ 2020; 369: m1067. [CrossRef] [Pubmed]
Lazarević D, Vojinović J. Immunoglobuline G4 (IgG4) deposit disease and orbital pseudotumor as first manifestations of Wegener’s granulomatosis (WG) in child. Ann Rheum Dis 2012; 71(suppl 3): 681. [CrossRef]
Ma Y, Chen L, Xu Y, Han Q, Yu B, Yuan Y, et al. Clinical and pathological features of patients with antineutrophil cytoplasmic antibody-associated vasculitides concomitant with IgG4-related disease. Int J Rheum Dis 2019; 22(12): 2143-50. [CrossRef] [Pubmed]
Maggina P, Askiti V, Maurikou M, Mila M, Papadatos D, Lela Stamogianou, et al. Orbital pseudotumor: A single precursor clinical manifestation of Wegener granulomatosis in a ten year old boy. O J Ped 2012; 2: 56-9. [CrossRef]
Maritati F, Peyronel F, Vaglio A. IgG4-related disease: a clinical perspective. Rheumatology (Oxford) 2020; 59(Suppl 3): iii123-31. [CrossRef] [Pubmed]
Matsuo T, Ichimura K, Sato Y, Tanimoto Y, Kiura K, Kanazawa S, et al. Immunoglobulin G4 (IgG4)-positive or negative ocular adnexal benign lymphoid lesions in relation to systemic involvement. J Clin Exp Hematopathol. 2010; 50: 129-42.[CrossRef] [Pubmed]
Muller K, Lin JH. Orbital granulomatosis with polyangiitis (Wegener granulomatosis): clinical and pathologic findings. Arch Pathol Lab Med 2014; 138(8): 1110-4. [CrossRef] [Pubmed]
Neild GH, Rodriguez-Justo M, Wall C, Connolly JO. Hyper-IgG4 disease: report and characterisation of a new disease. BMC Med 2006; 4: 23-41. [CrossRef] [Pubmed]
Ozen S, Pistorio A, Lusan MS, Bakkaloglu A, Herlin T, Brik R, et al. EULAR/PRINTO/PRES criteria for Henoch-Schonlein purpura, childhood polyarteritis nodosa, childhood Wegener granulomatosis and childhood Takayasu arteritis: Ankara 2008. Part II: Final clasification criteria. Ann Rheum Dis 2010; 69: 798-806. [CrossRef] [Pubmed]
Provenzale JM, Mukherji S, Allen NB, Castillo M, Weber AW. Orbital involvement by Wegener’s Granulomatosis: imaging findings. Am J Roentgenol 1996; 166: 929-34. [CrossRef] [Pubmed]
Savino G, Campana A, Petrone G, Grimaldi G, Murchison AP. In search of a disease. Surv Ophthalmol 2017; 62(5): 716-21. [CrossRef] [Pubmed]
Smerla RG, Rontogianni D, Fragoulis GE. Ocular manifestations of IgG4-related disease in children. More common than anticipated? Review of the literature and case report. Clin Rheumatol 2018; 37(6): 1721-7. [CrossRef] [Pubmed]
Stone JH, Zen Y and Deshpande V. IgG4-related disease. N Engl J Med 2012; 366: 539-51. [CrossRef] [Pubmed]
Twilt M, Benseler S. Childhood antineutrophil cytoplasmic antibodies associated vasculitides. Curr Opin Rheumatol 2014; 26: 50-5. [CrossRef] [Pubmed]
Vanwynsberghe D, Van den Broecke C, Bauters W, Decock C. Ocular presentation of Wegener granulomatosis. Bull Soc belge Ophtalmol 2007; 303: 7-11. [Pubmed]
Wallace ZS, Naden RP, Chari S, Choi H, Della‐Torre E, Dicaire JF, et al. The 2019 American college of rheumatology/European league against rheumatism classification criteria for IgG4‐related disease. Arthritis Rheumatol 2020; 72(1): 7-19. [CrossRef] [Pubmed]